Nucleic Acid Purification Cartridge

Abstract

A microfluidic device is disclosed having an enclosed chamber containing a filter for purifying biological or chemical analytes from a complex biological sample, said chamber housing a plurality of ports in addition to said filter, as follows: a first port enabling gas communication of the chamber with a vacuum generator, via a first flow path; a second port enabling liquid communication of the chamber with one or more reservoirs, via a second flow path; a third port enabling gas and liquid communication of the chamber with both one or more receiving containers and a vacuum generator, via a third flow path; and a filter located between the third port and both the first and second port, so that a fluid entering the chamber through the first and/or second port and exiting the chamber through the third port flows through the filter. The invention also relates to a method using the microfluidic device.

Claims

1.-17. (canceled)

18. A microfluidic device comprising: one or more reservoirs; one or more receiving containers; a purification cavity configured to be detachable from the microfluidic device, the purification cavity comprising: a first port configured to provide gas communication between the purification cavity and a vacuum generator, via a first flow path; a second port configured to provide liquid communication between the purification cavity and the one or more reservoirs, via a second flow path; and a third port configured to provide gas and liquid communication between the purification cavity and both the one or more receiving containers and the vacuum generator, via a third flow path; and a filter configured to purify biological or chemical analytes from a complex biological sample and located over the third port such that fluid entering the purification cavity through the first or second port and exiting the purification cavity through the third port flows through the filter.

19. The microfluidic device of claim 18, wherein the microfluidic device is a microfluidic cartridge and is designed to be disposable.

20. The microfluidic device of claim 18, wherein the microfluidic device is a microfluidic cartridge and is reusable.

21. The microfluidic device of claims 18, wherein the analytes comprise nucleic acids.

22. The microfluidic device of claim 18, wherein the filter comprises silica.

23. The microfluidic device of claim 22, wherein the filter comprises a silica membrane.

24. The microfluidic device of claim 22, wherein the filter comprises a resin containing silica beads.

25. The microfluidic device of claim 5, wherein the filter comprises a resin containing silica-coated beads.

26. The microfluidic device of claim 18, wherein the purification cavity comprises a clipping feature configured to fix the position of the purification cavity in the microfluidic device.

27. The microfluidic device of claim 18, wherein the vacuum generator is a syringe pump, a diaphragm pump, or a combination of the two.

28. The microfluidic device of claim 18, further comprising a first pressure sensor located within the third flow path between the purification cavity and the one or more receiving containers.

29. The microfluidic device of claim 28, further comprising a second pressure sensor located within the first flow path between the purification cavity and the vacuum generator.

30. The microfluidic device of claim 18, further comprising one or more multiport valves coupled to each of the first flow path, second flow path, and third flow path.

31. The microfluidic device of claim 30, wherein the one or more multiport valves are triggered by a pressure difference.

32. The microfluidic device of claim 30, wherein a dead volume enclosed by the third flow path between its corresponding one or more multiport valves and the filter is between 1 μL and 10 mL.

33. A method of purifying a biological or chemical analyte from a complex biological sample using the microfluidic device according to claim 1, the method comprising the steps of: applying a negative pressure difference between the purification cavity and a first reservoir to flow a liquid sample into the purification cavity through the second port; applying a negative pressure difference between a first receiving container and the purification cavity to flow the liquid sample through the filter and out the third port; and eluting the analyte from the filter by applying a negative pressure difference between the purification cavity and a second receiving container to flow an elution buffer through the filter and out the third port.

34. The method of claim 33, wherein the eluting further comprises: applying a negative pressure difference between the purification cavity and a second reservoir to flow the elution buffer into the purification cavity through the second port; and incubating the elution buffer with the filter for a predetermined incubation time.

35. The method of claim 33, further comprising incubating the liquid sample with the filter for a predetermined incubation time.

36. The method of claim 33, further comprising applying a negative pressure between the vacuum generator and the purification cavity via the third port to flow gas through the filter.

37. The method of claim 33, further comprising applying a negative pressure difference between a third reservoir and the first receiving container to flow a washing buffer located in the third reservoir through the second port of the purification cavity and out the third port of the purification cavity.

Description

FIGURE CAPTIONS

[0046] FIG. 1 shows a purification column (1) from a commercial kit for manual purification consisting of a plastic body (2) and a membrane filter (3) compressed and held in place by a fixation ring (10). The plastic body comprises a liquid inlet (4) and a liquid outlet (5).

[0047] FIG. 2A shows part of a microfluidic device (100) with an integrated purification cavity (101), and a membrane filter (3) held in place by a fixation ring (10).

[0048] FIG. 2B shows a rotated view for the microfluidic device (100) with an integrated purification cavity (101), and a membrane filter (3) held in place by a fixation ring (10). The gas port (102), liquid inlet port (103) and outlet port (104) connected to the purification cavity (101) are also shown.

[0049] FIG. 2C shows a separate purification cavity (200).

[0050] FIG. 2D shows a purification cavity (200) assembled in a microfluidic device (100). The clipping feature (201) holds the purification cavity (200) in place and applies the right compression to the membrane filter (3). The gas port (203), liquid inlet port (204) and outlet port (205) are also shown.

[0051] FIG. 2E illustrates the port configuration and the flow direction during loading of liquid (STEP 1) and washing/elution (STEP 2). Solid arrow indicates liquid flow; dotted arrow indicates gas flow; X indicates port closed by valve.

[0052] FIGS. 3 to 11: Detailed fluidic diagrams showing the port/valve configuration for each of the steps detailed in table 1. It is to be understood that the device of the present invention may but does not necessarily comprise each of the elements shown in the figures. The description and/or claims denote the essential elements. In addition to said elements one or more further optional elements may be independently chosen from each other. The optional elements are indicated in the following. 1: vacuum generator 1 (e.g. syringe pump); 2: vacuum generator 2 (optional, e.g. diaphragm pump); 3-7: valves (e.g. multiport valves); 8 and 9: pressure sensors (optional); 10: chamber; 11: fixation ring (optional); 12: filter; 13: waste receiving container (optional); 14: eluate receiving container; 15: sample reservoir; 16-17: reservoirs (optional); 18: elution buffer reservoir.